1,4-Benzenediboronic acid, 96%
1,4-Benzenediboronic acid, 96%
1,4-Benzenediboronic acid, 96%
Thermo Scientific Chemicals

1,4-Benzenediboronic acid, 96%

CAS: 4612-26-4 | C6H8B2O4 | 165.746 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
25 g
Catalog number B24064.06
also known as B24064-06
Price (EUR)
126,00
Each
Quantity:
5 g
Request bulk or custom format
Price (EUR)
126,00
Each
Chemical Identifiers
CAS4612-26-4
IUPAC Name[4-(dihydroxyboranyl)phenyl]boronic acid
Molecular FormulaC6H8B2O4
InChI KeyBODYVHJTUHHINQ-UHFFFAOYSA-N
SMILESOB(O)C1=CC=C(C=C1)B(O)O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream
Identification (FTIR)Conforms
Assay (Aqueous acid-base Titration)≥95.0%
Proton NMRConforms to structure
Assay (HPLC)≥95.0%
View more
It is used for palladium-catalyzed sequential alkenylation and conjugate addition reactions, scholl cyclizations, Suzuki-Miyaura cross-coupling reactions. It is also used in the preparation of indolizine derivatives as OLEDs, in organic thin-film transistors, Fluorescence and solution-processable coordination polymers.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used for palladium-catalyzed sequential alkenylation and conjugate addition reactions, scholl cyclizations, Suzuki-Miyaura cross-coupling reactions. It is also used in the preparation of indolizine derivatives as OLEDs, in organic thin-film transistors, Fluorescence and solution-processable coordination polymers.

Solubility
Soluble in water 2.5%.

Notes
Store in a cool, dry place in tightly closed container. Store at room temperature. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Byung Seok Kim; Sun Young Lee; So Won Youn. Pd-catalyzed sequential C-C and C-N bond formations for the synthesis of N-heterocycles: exploiting protecting group-directed C-H activation under modified reaction conditions. Chemistry An Asian Journal. 2011, 6 (8), 1952-1957.
  2. Supratim Basak; Pramiti Hui; Sathyanarayana Boodida; Rajadurai Chandrasekar. Micropatterning of metallopolymers: syntheses of back-to-back coupled octylated 2,6-bis(pyrazolyl)pyridine ligands and their solution-processable coordination polymers. Journal of Organic Chemistry. 2012, 77 (7), 3620-3626.